A short diastereoselective synthesis of orthogonally protected diaminosuccinic acid derivatives.
Kirsten Zeitler, Wolfgang Steglich
Index: J. Org. Chem. 69(18) , 6134-6, (2004)
Full Text: HTML
Abstract
Homogeneous, Rh-catalyzed hydrogenation of heteromeric olefinic glycine dimers presents an efficient route to diastereomerically pure, orthogonally protected diaminosuccinic acid derivatives depending on the double bond geometry of the starting material. The products were obtained as racemates.
Related Compounds
Related Articles:
2007-08-10
[J. Chromatogr. A. 1160(1-2) , 246-53, (2007)]
1981-07-01
[Eur. J. Biochem. 117(3) , 635-8, (1981)]
2004-03-01
[J. Pept. Res. 63(3) , 196-9, (2004)]
1994-01-01
[Basic Life Sci. 63 , 155-66, (1994)]